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异氟烷对神经肌肉阻滞剂作用于肌肉烟碱型乙酰胆碱受体的影响。

Effects of isoflurane on the actions of neuromuscular blockers on the muscle nicotine acetylcholine receptors.

作者信息

Li Chuanxiang, Yao Shanglong, Nie Hui, Lü Bin

机构信息

Department of Anesthesiology, Union Hospital, Tongji Medical College. Huazhong University of Science and Technology, Wuhan 430022, China.

出版信息

J Huazhong Univ Sci Technolog Med Sci. 2004;24(6):605-6, 614. doi: 10.1007/BF02911369.

Abstract

In this study, we tested the hypothesis that volatile anesthetic enhancement of muscle relaxation is the result of combined drug effects on the nicotinic acetylcholine receptors. The poly A m RNA from muscle by isolation were microinjected into Xenopus oocytes for receptor expression. Concentration-effect curves for the inhibition of Ach-induced currents were established for vecuronium, rocuranium, and isoflurane. Subsequently, inhibitory effects of NDMRs were studied in the presence of the isoflurane at a concentration equivalent to half the concentration producing a 50% inhibition alone. All tested drugs produced rapid and readily reversible concentration-dependent inhibition. The 50% inhibitory concentration values were 889 micromol/L (95% CI: 711-1214 micromol). 33.4 micromol (95% CI: 27.1-41.7 nmol) and 9.2 nmol (95% CI: 7.9-12.3 nmol) for isoflurane. rocuranium and vecuronium, respectively. Coapplication of isoflurane significantly enhanced the inhibitory effects of rocuranium and vecuronium, and it was especially so at low concentration of NMDRs. Isoflurane increases the potency of NDMRs, possibly by enhancing antagonist affinity at the receptor site.

摘要

在本研究中,我们检验了以下假设:挥发性麻醉药增强肌肉松弛作用是药物对烟碱型乙酰胆碱受体产生联合效应的结果。通过分离获取肌肉中的多聚腺苷酸mRNA,并将其显微注射到非洲爪蟾卵母细胞中以进行受体表达。建立了维库溴铵、罗库溴铵和异氟烷对乙酰胆碱诱导电流抑制作用的浓度-效应曲线。随后,在异氟烷浓度相当于单独产生50%抑制作用浓度一半的情况下,研究了非去极化肌松药的抑制作用。所有受试药物均产生快速且易于逆转的浓度依赖性抑制作用。异氟烷、罗库溴铵和维库溴铵的50%抑制浓度值分别为889微摩尔/升(95%可信区间:711 - 1214微摩尔/升)、33.4纳摩尔(95%可信区间:27.1 - 41.7纳摩尔)和9.2纳摩尔(95%可信区间:7.9 - 12.3纳摩尔)。异氟烷与罗库溴铵和维库溴铵联合应用时,显著增强了它们的抑制作用,在低浓度非去极化肌松药时尤其如此。异氟烷可能通过增强受体部位拮抗剂的亲和力来提高非去极化肌松药的效能。

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